Canonical Allele Identifier: PA2826463248
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408529
ClinVar RCV Id: RCV002230809

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Lys182Asn
CA16610847
NM_001258281.1:c.546A>C
CA346732288
NM_001258281.1:c.546A>T